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rs786205538

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205538(C;T)
Make rs786205538(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178552677
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs786205538
ebirs786205538
HLIrs786205538
Exacrs786205538
Varsomers786205538
Maprs786205538
PheGenIrs786205538
hapmaprs786205538
1000 genomesrs786205538
hgdprs786205538
ensemblrs786205538
gopubmedrs786205538
geneviewrs786205538
scholarrs786205538
googlers786205538
pharmgkbrs786205538
gwascentralrs786205538
openSNPrs786205538
23andMers786205538
23andMe allrs786205538
SNP Nexus

SNPshotrs786205538
SNPdbers786205538
MSV3drs786205538
GWAS Ctlgrs786205538
Max Magnitude0
ClinVar
Risk rs786205538(T;T)
Alt rs786205538(T;T)
Reference rs786205538(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179417404G>A
CLNSRC
CLNACC RCV000171312.1,